🔎 Trials Near Me

Home › Breast Cancer › NCT06246968

A Study of Pembrolizumab and Ablation (Cryoablation or Histotripsy) in People With Breast Cancer

RecruitingPhase 1

Does Ablation (Cryoablation or Histotripsy) Boost Immune Response Improving the Benefits of Pembrolizumab in Patients With Metastatic or Locally Advanced Triple Negative Breast Cancer?

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

* Patients ≥ 18 years of age
* Confirmed histologic diagnosis of metastatic TNBC or locally advanced inoperable TNBC
* 1 site amenable cryoablation of at least 1.5 cm in size as determined by an Interventional Radiologist. Eligible cryoablation sites include (but not limited to) soft tissue, liver, lung, and bone as determined by an Interventional Radiologist to be safest and most feasible.
* Physically fit (clinically eligible) to undergo ablation as per usual clinical practice
* Per clinical guidelines, women of childbearing age should use effective contraception during treatment with pembrolizumab and for at least 4 months after the last dose of the drug, which will be assessed and monitored by, and the responsibility of, the patient's medical oncologist (not study investigators or research team) as pembrolizumab is standard of care. Memorial Sloan Kettering Cancer Center Pregnancy Standards will be followed prior to ablation. That is, female patients that are 11-50 years of age and of childbearing potential will undergo a pregnancy test within 2 weeks (15 days) before ablation. Pregnancy test will not be required in patients with bilateral oophorectomy, bilateral salpingectomy, bilateral salpingectomy-oophorectomy, hysterectomy, menopause (no menses ≥ 1 year prior to treatment or after completion of all treatment), or surgical sterilization (i.e. tubal ligation or blockage), with documentation of permanent exemptions in CIS ("Pregnancy Testing Exemption").
* Pembrolizumab therapy (200 mg every 3 weeks) planned as part of standard of care as first, second, or third line of therapy

  * Eligible for PD-1 inhibitor per the patient's medical oncologist, with planned treatment with PD-1 inhibitor per the patient's medical oncologist. Additional systemic therapy is per the patient's medical oncologist. The following systemic therapy will be accepted (the timing of the systemic therapy relative to pembrolizumab and ablation is not restricted):

    * Capecitabine (Xeloda, available as a generic drug)
    * Carboplatin (Paraplatin, available as a generic drug)
    * Cisplatin (Platinol, available as a generic drug)
    * Cyclophosphamide (Cytoxan, available as a generic drug)
    * Docetaxel (Taxotere)
    * Doxorubicin (Adriamycin, available as a generic drug)
    * Pegylated liposomal doxorubicin (Doxil)
    * Epirubicin (Ellence, available as a generic drug)
    * Eribulin (Halaven)
    * Fluorouracil (5-FU, Adrucil, available as a generic drug)
    * Gemcitabine (Gemzar, available as a generic drug)
    * Ixabepilone (Ixempra)
    * Methotrexate (available as a general drug)
    * Nab-paclitaxel (Abraxane)
    * Paclitaxel (Taxol, available as a generic drug)
    * Vinorelbine (Navelbine, available as a generic drug)

Exclusion Criteria:

* Patient not eligible for PD-1 inhibitor per the patient's medical oncologist
* No disease amenable for ablation
* Pembrolizumab therapy not planned as part of standard of care

About the study

Participants will have a confirmed diagnosis of metastatic breast cancer and will receive pembrolizumab in combination with ablation (cryoablation or histotripsy) OR pembrolizumab alone. Participants will be randomly assigned.

What is being tested

Sponsor: Memorial Sloan Kettering Cancer Center · Participants: 30 · Started: Jan 29, 2024

Contact the study team

Official record on ClinicalTrials.gov — NCT06246968

Locations in the U.S.

New JerseyMemorial Sloan Kettering Cancer Center at Basking Ridge (Limited Protocol Activities), Basking Ridge
Memorial Sloan Kettering Monmouth (Limited protocol activities), Middletown
Memorial Sloan Kettering Bergen (Limited Protocol Activities), Montvale
New YorkMemorial Sloan Kettering Suffolk-Commack (Limited Protocol Activities ), Commack
Memorial Sloan Kettering Westchester (Limited Protocol Activities), Harrison
Memorial Sloan Kettering Cancer Center (All protocol activites), New York
Memorial Sloan Kettering Nassau (Limited Protocol Activites), Rockville Centre

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.